HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Isopropylpiperidin-4-yl)methanamine → 2-Chloropropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Isopropylpiperidin-4-yl)methanamine | HCID 7258859 | — |
| Reactant | 3-Chloro-6-chlorocarbonylphenylsulfenyl chloride | HCID 10728826 | — |
| Product | 2-Chloropropane | HCID 6361 | — |
| Product | N-(piperidin-4-ylmethyl)acetamide | HCID 4341747 | — |
Reaction Steps
2-(1-isopropylpiperid-4-ylmethyl)-6-chloro-1,2-benzisothiazolin-3-one is obtained analogously to Example 33 by reacting 3-chloro-6-chlorocarbonylphenylsulfenyl chloride and 1-isopropyl-4-aminomethylpiperidine [boiling point 15: 95°-97° C.; obtained from 4-acetylaminomethylpiperidine and isopropyl chloride analogously to Singh et al., J. Med. Chem. 12, 949 (1969) and Werbel et al., supra]. After recrystallization in acetone, yellow crystals of melting point 134°-135° C. are obtained; yield: 37% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04190663 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-aeae6fcd82d04f3aaad0ba67c05d7052 |
| Source note | uspto-grants-1980_02 |