TERT-BUTYLCARBAMIDINE HYDROCHLORIDE
TERT-BUTYLCARBAMIDINE HYDROCHLORIDE Basic information
- Product Name:
- TERT-BUTYLCARBAMIDINE HYDROCHLORIDE
- Synonyms:
-
- 2,2-DIMETHYLPROPANIMIDAMIDE HYDROCHLORIDE
- 2,2-DIMETHYLPROPIONAMIDINE HCL
- 2,2-DIMETHYL-PROPIONAMIDINEHYDROCHLORIDE
- TERT-BUTYLCARBAMIDINE HYDROCHLORIDE
- T-BUTYLCARBAMIDINE HYDROCHLORIDE
- tert-ButylcarbamidineHCl
- trimethylacetamidine hydrochloride
- pivalamidine hydrochloride
- CAS:
- 18202-73-8
- MF:
- C5H13ClN2
- MW:
- 136.62
- EINECS:
- 242-091-1
- Product Categories:
-
- pharmacetical
- Aliphatics
- Mol File:
- 18202-73-8.mol
TERT-BUTYLCARBAMIDINE HYDROCHLORIDE Chemical Properties
- Melting point:
- 190 °C
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- powder to crystal
- color
- White to Almost white
- Sensitive
- Hygroscopic
- BRN
- 3618865
- InChIKey
- ARDGQYVTLGUJII-UHFFFAOYSA-N
- CAS DataBase Reference
- 18202-73-8(CAS DataBase Reference)
MSDS
- Language:English Provider:ALFA
TERT-BUTYLCARBAMIDINE HYDROCHLORIDE Usage And Synthesis
Uses
Pivalimidamide Hydrochloride is used as a reagent in the preparation of 2-alkyl-4-aryltetrahydropyridopyrimidines and 2-alkyl-4-aryl-tetrahydropyrimidoazepines as selective 5-HT2A antagonists.
Synthesis
630-18-2
75-36-5
18202-73-8
Step (1) Preparation of tert-butylamidine hydrochloride: To a magnetically stirred mixed solution of 2,2-dimethyl-1-propanenitrile (25.0 g, 0.30 mol) and anhydrous methanol (26.8 mL, 0.79 mol) was added dropwise acetyl chloride (25 mL, 0.36 mol) and ether (30 mL) at 0 °C. After the dropwise addition, stirring was continued at 0 °C for 15 min. Subsequently, the reaction mixture was stirred at room temperature for 3 days. After completion of the reaction, white crystals were obtained by filtration, washed with ether and dried under vacuum. The dried crystals were mixed with an ethanol solution of 10% ammonia (150 mL, 0.90 mol) and stirred at room temperature for 3 days. The reaction mixture was filtered and the filtrate was concentrated to give a white solid. Recrystallization by ethanol gave a white crystalline product (18.9 g, 46% yield) with a melting point of 205°C (literature value 188°-190°C). NMR hydrogen spectrum (DMSO-d6): δ 1.22 (s, 9H), 8.63 (br d, 3H).
References
[1] Patent: US4786640, 1988, A
TERT-BUTYLCARBAMIDINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materials
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TERT-BUTYLCARBAMIDINE HYDROCHLORIDE(18202-73-8)Related Product Information
- Dimethylamine
- 2,2-DIMETHYLPROPIONAMIDINE
- 1-Methyl-cyclopropanecarboxamidine HCl
- 1-(2,4-dichlorophenyl)cyclopropanecarboxamidine
- PIVALIMIDOHYDRAZIDE HYDROCHLORIDE
- ADAMANTANE-1-CARBOXAMIDINE HYDROCHLORIDE
- 5,5-Diethyl-4-(2-chlorophenyl)iminobarbituric acid
- N,N-DIMETHYL-[1-T-BUTYL-3,3-BIS(DIMETHYLAMINO)-2-AZA-3-PROPENYLIDEN]-AMMONIUM PERCHLORATE
- PYRIDO[3,4-D]PYRIMIDIN-4(3H)-ONE, 6-CHLORO-2-(1,1-DIMETHYLETHYL)-
- 1-(4-chlorophenyl)cyclopropanecarboxamidine
- TERT-BUTYLCARBAMIDINE HYDROCHLORIDE